Copper catalyzed C(sp<sup>3</sup>)–H/C(sp<sup>3</sup>)–H cross-coupling of arylacetic acid equivalents with methylarenes <i>via</i> α-carbonyl radicals

Arylacetic acid equivalents bearing a pyridine group undergo C(sp<sup>3</sup>)-H/C(sp<sup>3</sup>)-H cross coupling with diverse methylarenes in the presence of a copper based catalyst system. The reaction proceeds <i>via</i> the formation of α-carbonyl radicals giving access to α,β-diarylpropionic acids. Preliminary study suggests that the catalyst system is capable of transforming arylbenzyl ketones into 1,2,3-triaryl ketones.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d4cc06801g
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81

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article

Copper catalyzed C(sp3)–H/C(sp3)–H cross-coupling of arylacetic acid equivalents with methylarenes via α-carbonyl radicals

Bishwajit Ganguly, Ashok Kumar Singh, Sukalyan Bhadra, Ajijur Rahaman et al.
3 citations
Chemical Communications
Catalytic C–H Functionalization Methods
2.81
article

Copper catalyzed C(sp3)–H/C(sp3)–H cross-coupling of arylacetic acid equivalents with methylarenes via α-carbonyl radicals

Bishwajit Ganguly, Ashok Kumar Singh, Sukalyan Bhadra, Ajijur Rahaman, Surjit Bhai, Tulsi R. Patel, Upendra Kumar Brijmohan Patel
article en
3 citations

Abstract

Arylacetic acid equivalents bearing a pyridine group undergo C(sp<sup>3</sup>)-H/C(sp<sup>3</sup>)-H cross coupling with diverse methylarenes in the presence of a copper based catalyst system. The reaction proceeds <i>via</i> the formation of α-carbonyl radicals giving access to α,β-diarylpropionic acids. Preliminary study suggests that the catalyst system is capable of transforming arylbenzyl ketones into 1,2,3-triaryl ketones.

Chemical CommunicationsVol. 61(14)
Central Salt and Marine Chemicals Research Institute (IN), Academy of Scientific and Innovative Research (IN)
Science and Engineering Research Board, Central Salt and Marine Chemicals Research Institute, Council of Scientific and Industrial Research
Openalex Percentile: Top 12%
Catalytic C–H Functionalization Methods
2.81
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